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Titlebook: Atlas of Cutaneous Lymphomas; Classification and D Joi B. Carter,Amrita Goyal,Lyn McDivitt Duncan Book 2015 Springer International Publishi

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41#
發(fā)表于 2025-3-28 16:24:45 | 只看該作者
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發(fā)表于 2025-3-28 19:10:41 | 只看該作者
Developing Learning Organizations, This indolent lymphoma is the second most common of all cutaneous T-cell lymphomas. It typically presents with solitary cutaneous and subcutaneous erythematous-to-violaceous papules and nodules. Although relapse after treatment is very common, patients are typically asymptomatic, and the vast major
43#
發(fā)表于 2025-3-28 23:13:35 | 只看該作者
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發(fā)表于 2025-3-29 06:09:05 | 只看該作者
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發(fā)表于 2025-3-29 08:44:21 | 只看該作者
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發(fā)表于 2025-3-29 11:41:00 | 只看該作者
The Rules of the Game Have Changed,provisional entity in the World Health Organization–European Organization for Research and Treatment of Cancer (WHO/EORTC) guidelines and is considered to have both indolent and aggressive forms. pcSMPTCL typically presents with a persistent, asymptomatic, solitary erythematous nodule or pink plaque
47#
發(fā)表于 2025-3-29 18:21:04 | 只看該作者
48#
發(fā)表于 2025-3-29 20:21:01 | 只看該作者
Allam Hamdan,Arezou Harraf,Hala Alsabatinors. It has an excellent prognosis. This entity has also been known as cutaneous marginal zone lymphoma (CMZL), extranodal marginal zone lymphoma of mucosa associated lymphoid tissue (MZL or MALT lymphoma), primary cutaneous immunocytoma, primary cutaneous plasmacytoma, and lymphoma cutis [1, 2]. Th
49#
發(fā)表于 2025-3-30 00:31:29 | 只看該作者
Sayda Ben Sghaier,Rafaa Mraihi,Arij Lahmarenter B cells constitutes 60 % of all primary cutaneous B-cell lymphomas and 9–11 % of all cutaneous lymphomas [1, 2]. It also includes 5 % of all follicular lymphomas, nodal and extranodal [3]. It typically presents with firm, erythematous to violaceous papules, plaques, and tumors on the scalp, tr
50#
發(fā)表于 2025-3-30 07:51:22 | 只看該作者
Quality Management System Audit,cally presents on the leg with erythematous or violaceous tumors or nodules, it can also present elsewhere on the body. Patients with pcDLBCL have a moderately poor prognosis and experience frequent systemic dissemination. Though small case series have reported dramatic improvements in survival with
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